| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45001471-45002140 | Common:3; Rare:215 | ||||
| chr19:45038942-45039100 | Rare:105 | ||||
| chr19:45039310-45039860 | Common:7; Rare:213 | ||||
| chr19:45076428-45076598 | Rare:53 | ||||
| chr19:45079142-45079317 | Common:1; Rare:77 | ||||
| chr19:45091639-45091828 | Common:1; Rare:53 | ||||
| chr19:45092816-45093232 | Common:6; Rare:242 | ||||
| chr19:45178195-45179010 | Common:15; Rare:294; Clinvar:1; Clinvar (benign):7 | ||||
| chr19:45250950-45251540 | Common:4; Rare:204 | ||||
| chr19:45370538-45370836 | Common:4; Rare:165 | ||||
| chr19:45405016-45405242 | Common:1; Rare:76 | ||||
| chr19:45405840-45406210 | Common:3; Rare:104 | ||||
| chr19:45406313-45406696 | Common:5; Rare:181 | ||||
| chr19:45423335-45423951 | Common:11; Rare:239; Clinvar (benign):3 | ||||
| chr19:45424366-45424597 | Common:2; Rare:31 |